SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease. - Wikidata - awgldk - TriplyDB

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.

http://www.wikidata.org/entity/Q33907034

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Current challenges in the bioinformatics of single cell genomics.Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis How many diseases does it take to map a gene with SNPs?Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma Comparison of the accuracy of methods of computational haplotype inference using a large empirical dataset Genetic epidemiology. Approaches to the genetic analysis of rheumatoid arthritis Genetic epidemiology: systemic sclerosis.Polyallelic structural variants can provide accurate, highly informative genetic markers focused on diagnosis and therapeutic targets: Accuracy vs. Precision Accessing genetic variation: genotyping single nucleotide polymorphisms Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis Exercise, APOE genotype, and the evolution of the human lifespan Genomic variants, genes, and pathways of Alzheimer's disease: An overview.Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.HapFABIA: identification of very short segments of identity by descent characterized by rare variants in large sequencing data.Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.Mining genetic epidemiology data with Bayesian networks I: Bayesian networks and example application (plasma apoE levels).Multipoint linkage disequilibrium mapping using multilocus allele frequency data.Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes.Haplotype reconstruction error as a classical misclassification problem: introducing sensitivity and specificity as error measures.CGTS: a site-clustering graph based tagSNP selection algorithm in genotype data Platelet cytochrome oxidase and citrate synthase activities in APOE ε4 carrier and non-carrier Alzheimer's disease patients.Genetic studies in human prion diseases.Haplotype information and linkage disequilibrium mapping for single nucleotide polymorphisms.GERBIL: Genotype resolution and block identification using likelihood.Sequence variation in IGF1R is associated with differences in insulin levels in nondiabetic Old Order Amish.The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity.A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other.Efficient multipoint linkage analysis through reduction of inheritance space.Haplotype analysis improved evidence for candidate genes for intramuscular fat percentage from a genome wide association study of cattle.Osteoprotegerin CGA haplotype protection against cerebrovascular complications in anti-CCP negative patients with rheumatoid arthritis Allelic association of the neuronal nitric oxide synthase (NOS1) gene with schizophrenia.Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.Family-based tests of association in the presence of linkage.A TOMM40 variable-length polymorphism predicts the age of late-onset Alzheimer's disease The relative power of SNPs and haplotype as genetic markers for association tests.Single nucleotide polymorphism seeking long term association with complex disease

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P2860

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.

http://www.wikidata.org/entity/Q33907034

description

2000 nî lūn-bûn

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2000 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2000 թվականի հունիսին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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American Journal of Human Genetics

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SNPing away at complex disease ...... und APOE in Alzheimer disease.

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A D Roses

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A J Afshari

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A R Rogala

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B D Slotterbeck

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D E Schmechel

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E R Martin

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J F Stevens

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J R Gilbert

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P2860

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage

Strategies for multilocus linkage analysis in humans

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

Sequencing of 42kb of the APO E-C2 gene cluster reveals a new gene: PEREC1

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

A DNA polymorphism discovery resource for research on human genetic variation

The future of genetic studies of complex human diseases

Real time quantitative PCR

Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease.

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383-394

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10.1086/303003

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2

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67

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Jeffery M. Vance

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25101997

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10869235

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Alzheimer's disease

single-nucleotide polymorphism

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